Date posted
Commute time
Locations
Type of Company
Job types
Locations
Filters
Sort byRelevance
Locations
Date posted
Type of Company
Job types
Locations
There is no job matching your search
Api
Suffolk
No need to fret! We’re adding new jobs every single day. Find out immediately when we’ve found a match for you.
1 exact match is outside your preferred location
)
Broad and expert knowledge of analytical methodologies supporting API development. The site includes state-of-the-art GMP facilities for API development, oral solid dose manufacture, formulation development, and process chemistry.
Broad and expert knowledge of analytical methodologies supporting API development. The site includes state-of-the-art GMP facilities for API development, oral solid dose manufacture, formulation development, and process chemistry.
These jobs might also interest you
)
As a Senior Scientist in Protein and Cell Sciences, you will design, express, purify and characterize recombinant proteins that underpin antibody discovery and other biologics programs. Are you ready to turn recombinant protein design into therapies that change the way cancer is treated? You will use modern computational tools alongside rigorous experimental methods to ensure the proteins you produce behave as intended. * Recombinant Antigen Design: Apply computational structural biology (including AlphaFold and ProteinMPNN) to design target proteins that are fit-for-purpose for discovery and development. * Protein Production: Express and purify recombinant proteins using bacterial and transient mammalian systems (E.coli, HEK, CHO), building robust, scalable methods and standard operating procedures that improve throughput and reproducibility.
As a Senior Scientist in Protein and Cell Sciences, you will design, express, purify and characterize recombinant proteins that underpin antibody discovery and other biologics programs. Are you ready to turn recombinant protein design into therapies that change the way cancer is treated? You will use modern computational tools alongside rigorous experimental methods to ensure the proteins you produce behave as intended. * Recombinant Antigen Design: Apply computational structural biology (including AlphaFold and ProteinMPNN) to design target proteins that are fit-for-purpose for discovery and development. * Protein Production: Express and purify recombinant proteins using bacterial and transient mammalian systems (E.coli, HEK, CHO), building robust, scalable methods and standard operating procedures that improve throughput and reproducibility.
NEW
)
Medpace is currently seeking candidates with Oncology PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. * Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). * Compile and maintain project-specific status reports within the clinical trial management system - Candidate must have a desire to transfer and apply analytical and academic skills in clinical ...
Medpace is currently seeking candidates with Oncology PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. * Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). * Compile and maintain project-specific status reports within the clinical trial management system - Candidate must have a desire to transfer and apply analytical and academic skills in clinical ...
NEW
)
Our client is looking for a Senior Development Scientist who has navigated the full journey from early-stage concept to commercially viable product - and wants to do it again, at pace, in a high-growth environment. You'll be a key member of the development team, responsible for shaping technical direction and driving delivery across the full product development lifecycle. * Provide day-to-day technical leadership and line management, developing the scientists around you * A clear track record of taking biological products or workflows from early development through to robust, commercially deployed solutions * Proven ability to lead, mentor, and manage scientists in a fast-moving commercial or industrial setting * Excellent communication skills, with the credibility to engage senior leadership and the clarity to support junior team members
Our client is looking for a Senior Development Scientist who has navigated the full journey from early-stage concept to commercially viable product - and wants to do it again, at pace, in a high-growth environment. You'll be a key member of the development team, responsible for shaping technical direction and driving delivery across the full product development lifecycle. * Provide day-to-day technical leadership and line management, developing the scientists around you * A clear track record of taking biological products or workflows from early development through to robust, commercially deployed solutions * Proven ability to lead, mentor, and manage scientists in a fast-moving commercial or industrial setting * Excellent communication skills, with the credibility to engage senior leadership and the clarity to support junior team members
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. * Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). * Compile and maintain project-specific status reports within the clinical trial management system - Candidate must have a desire to transfer and apply analytical and academic skills in clinical project ...
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. * Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). * Compile and maintain project-specific status reports within the clinical trial management system - Candidate must have a desire to transfer and apply analytical and academic skills in clinical project ...
NEW
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience in nuclear medicine, medical physics, medical imaging / radiopharmaceuticals or / radiation oncology for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will work with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. * Communicate and collaborate on global study activities; working closely with the Project Coordinator and Clinical Trial Manager Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). * Compile and maintain project-specific status reports within the clinical trial management system
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience in nuclear medicine, medical physics, medical imaging / radiopharmaceuticals or / radiation oncology for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will work with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. * Communicate and collaborate on global study activities; working closely with the Project Coordinator and Clinical Trial Manager Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). * Compile and maintain project-specific status reports within the clinical trial management system
NEW
)
Senior Quality Assurance Officer to join our Quality Assurance team on a 12 month fixed-term contract. In this role, you will?provide expert QA support for OXB Manufacturing Operations, playing a key part in advancing our mission and making a real difference. * Supporting manufacturing teams as a QA partner to ensure GMP compliance during production activities. OXB is a quality and innovation-led viral vector CDMO that enables its clients to deliver life-changing therapies to patients around the world. One of the original pioneers in cell and gene therapy, OXB has more than 30 years of experience in viral vectors, the driving force behind the majority of gene therapies. Cell and gene therapy is the treatment of disease by the delivery of therapeutic genetic material (DNA or RNA), into a patients cells. One highly effective approach to delivering genetic information is to re-engineer ...
Senior Quality Assurance Officer to join our Quality Assurance team on a 12 month fixed-term contract. In this role, you will?provide expert QA support for OXB Manufacturing Operations, playing a key part in advancing our mission and making a real difference. * Supporting manufacturing teams as a QA partner to ensure GMP compliance during production activities. OXB is a quality and innovation-led viral vector CDMO that enables its clients to deliver life-changing therapies to patients around the world. One of the original pioneers in cell and gene therapy, OXB has more than 30 years of experience in viral vectors, the driving force behind the majority of gene therapies. Cell and gene therapy is the treatment of disease by the delivery of therapeutic genetic material (DNA or RNA), into a patients cells. One highly effective approach to delivering genetic information is to re-engineer ...
NEW
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. * Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). * Compile and maintain project-specific status reports within the clinical trial management system - Candidate must have a desire to transfer and apply analytical and academic skills in clinical project ...
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. * Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). * Compile and maintain project-specific status reports within the clinical trial management system - Candidate must have a desire to transfer and apply analytical and academic skills in clinical project ...
NEW
We're looking for a Senior Development Scientist to join our client's team and help shape the next generation of protein science. Are you a protein scientist with a passion for translating cutting-edge biology into real-world products? * Apply protein characterisation techniques - such as HPLC/FPLC, mass spectrometry, or related analytical methods - to inform and accelerate product development You'll lead the design and optimisation of protein-based assays and workflows - from early feasibility through to robust, scalable solutions ready for commercial deployment. Drawing on your expertise in protein characterisation, you'll generate high-quality, well-controlled data that drives strategic decisions and moves prototypes into reliable, reproducible platform-integrated tools. * Lead and mentor a team of scientists, providing day-to-day technical guidance and line management
We're looking for a Senior Development Scientist to join our client's team and help shape the next generation of protein science. Are you a protein scientist with a passion for translating cutting-edge biology into real-world products? * Apply protein characterisation techniques - such as HPLC/FPLC, mass spectrometry, or related analytical methods - to inform and accelerate product development You'll lead the design and optimisation of protein-based assays and workflows - from early feasibility through to robust, scalable solutions ready for commercial deployment. Drawing on your expertise in protein characterisation, you'll generate high-quality, well-controlled data that drives strategic decisions and moves prototypes into reliable, reproducible platform-integrated tools. * Lead and mentor a team of scientists, providing day-to-day technical guidance and line management
Clinical Trial Managers with expertise in Oncology or other therapy areas are welcome to continue to work in their area of expertise or to expand to a new therapeutic area. Medpace is the leading CRO for Biotech companies and is continuing to add a Director of Clinical Trial Management (Operational role) to join our Clinical Trial Management Group in London, UK. * Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables * Minimum of 5 years of Clinical Trial Management experience, CRO experience preferred; We offer a very competitive salary/bonus program, plus equity grants which have become very lucrative for our associates. Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Job Summary
Clinical Trial Managers with expertise in Oncology or other therapy areas are welcome to continue to work in their area of expertise or to expand to a new therapeutic area. Medpace is the leading CRO for Biotech companies and is continuing to add a Director of Clinical Trial Management (Operational role) to join our Clinical Trial Management Group in London, UK. * Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables * Minimum of 5 years of Clinical Trial Management experience, CRO experience preferred; We offer a very competitive salary/bonus program, plus equity grants which have become very lucrative for our associates. Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Job Summary
NEW
Product Development Scientist
Product Development Scientist
Premier Recruitment Group Limited
Dartford (DA1)
£30000 - £32000 per annum + plus 5% bonus
As part of the assigned projects, the Product Development Scientist participates in the development of new diagnostics products and / or the technological improvement of existing products, from the feasibility phase to the launch phase, in compliance with the design requirements and the procedures of the Quality System. We are recruiting for experienced and forward thinking Product Development Scientist. * Participates in the various phases of the product development process, within the scope of the tasks assigned by the Team Manager; * Guarantees completion, availability of the product documentation relating to the assigned activities; * Collaborate in the definition and testing phase of new raw materials / technological innovations of products and processes; * Troubleshoot any issues arising from existing products;
As part of the assigned projects, the Product Development Scientist participates in the development of new diagnostics products and / or the technological improvement of existing products, from the feasibility phase to the launch phase, in compliance with the design requirements and the procedures of the Quality System. We are recruiting for experienced and forward thinking Product Development Scientist. * Participates in the various phases of the product development process, within the scope of the tasks assigned by the Team Manager; * Guarantees completion, availability of the product documentation relating to the assigned activities; * Collaborate in the definition and testing phase of new raw materials / technological innovations of products and processes; * Troubleshoot any issues arising from existing products;
)
Our client has expanded their Clinical Pharmacy & Safety Sciences operations to enable 7-day science, and they're looking for an experienced Research Technician to play a critical role in keeping discovery research moving while the rest of the week slows down. This role is ideal for a confident, detail-oriented Research Technician who enjoys owning their work and making a visible impact. This is a hands-on, laboratory-based role where your expertise directly supports cutting-edge research. * Work within a dynamic research environment * Make a meaningful impact - your work keeps critical research running - Location: Cambridge - Working Pattern: Friday to Monday | Weekend Shift - Ever felt like a Monday-to-Friday lab routine just isn't your thing? Good news - science doesn't stop at the weekend, and neither do we. If you enjoy independence, responsibility, and a work pattern that gives you your weekdays ...
Our client has expanded their Clinical Pharmacy & Safety Sciences operations to enable 7-day science, and they're looking for an experienced Research Technician to play a critical role in keeping discovery research moving while the rest of the week slows down. This role is ideal for a confident, detail-oriented Research Technician who enjoys owning their work and making a visible impact. This is a hands-on, laboratory-based role where your expertise directly supports cutting-edge research. * Work within a dynamic research environment * Make a meaningful impact - your work keeps critical research running - Location: Cambridge - Working Pattern: Friday to Monday | Weekend Shift - Ever felt like a Monday-to-Friday lab routine just isn't your thing? Good news - science doesn't stop at the weekend, and neither do we. If you enjoy independence, responsibility, and a work pattern that gives you your weekdays ...
FEATURED
Train new Clinical Safety Coordinators on safety reporting responsibilities - As such, we are searching for motivated individuals to join our Clinical Safety team in London. * SAE reconciliation between safety database and clinical database * Preparation of clinical safety documents as required (i.e., safety management plan, periodic safety reports and presentations) * Provide periodic safety summaries to project Data Manager, Clinical Trial Manager, and Medical Monitor * Demonstrate advanced knowledge of medical terminology, global safety reporting requirements and Good Clinical Practice (GCP) Guidelines - Working as part of a high performing group alongside Medical Monitors, Quality Assurance, Clinical Trial Management and others, this position plays a key role at Medpace to accomplish tasks and work on projects that are instrumental to the development of life changing medicines.
Train new Clinical Safety Coordinators on safety reporting responsibilities - As such, we are searching for motivated individuals to join our Clinical Safety team in London. * SAE reconciliation between safety database and clinical database * Preparation of clinical safety documents as required (i.e., safety management plan, periodic safety reports and presentations) * Provide periodic safety summaries to project Data Manager, Clinical Trial Manager, and Medical Monitor * Demonstrate advanced knowledge of medical terminology, global safety reporting requirements and Good Clinical Practice (GCP) Guidelines - Working as part of a high performing group alongside Medical Monitors, Quality Assurance, Clinical Trial Management and others, this position plays a key role at Medpace to accomplish tasks and work on projects that are instrumental to the development of life changing medicines.
NEW
As a Sample Dispatch Technician, you will be responsible for the end-to-end coordination of sample shipments globally, ensuring accuracy, compliance, and efficiency across all dispatch activities. We are partnering with a key player in the life sciences sector, offering an exciting opportunity for a Sample Dispatch Technician to join a highly regulated scientific operations environment. * Act as a point of contact for internal teams, external stakeholders, and customers regarding sample dispatch queries - This role focuses on the global shipment of R&D samples, ensuring all materials-biological, chemical, or radioactive-are handled, prepared, and shipped in full compliance with international transport and regulatory requirements. * Receive, accept, store, and manage samples, ensuring accurate documentation and compliance with Dangerous Goods and transport regulations
As a Sample Dispatch Technician, you will be responsible for the end-to-end coordination of sample shipments globally, ensuring accuracy, compliance, and efficiency across all dispatch activities. We are partnering with a key player in the life sciences sector, offering an exciting opportunity for a Sample Dispatch Technician to join a highly regulated scientific operations environment. * Act as a point of contact for internal teams, external stakeholders, and customers regarding sample dispatch queries - This role focuses on the global shipment of R&D samples, ensuring all materials-biological, chemical, or radioactive-are handled, prepared, and shipped in full compliance with international transport and regulatory requirements. * Receive, accept, store, and manage samples, ensuring accurate documentation and compliance with Dangerous Goods and transport regulations
FEATURED
)
This senior position has a three-year term with a leading research institution and has strong Data Science elements. As a PhD-qualified scientist with further research or commercial experience, you will bring your prior experience in signal processing to bear. * Additional experience in research or commercial R&D (including a leading/mentoring role in some capacity, either for a small team, research project, or supervising PhDs, etc.) The role comes with opportunities for collaborative research into a range of new areas, learning and applying new techniques whilst building your reputation through contributions and publications. R&D applying AI and algorithms to real-world signals/comms, sensor fusion - London, hybrid working; to £58k plus benefits - You'll be helping to establish and further the state of the art, with a view to paving the way for future technology adoption and new applications.
This senior position has a three-year term with a leading research institution and has strong Data Science elements. As a PhD-qualified scientist with further research or commercial experience, you will bring your prior experience in signal processing to bear. * Additional experience in research or commercial R&D (including a leading/mentoring role in some capacity, either for a small team, research project, or supervising PhDs, etc.) The role comes with opportunities for collaborative research into a range of new areas, learning and applying new techniques whilst building your reputation through contributions and publications. R&D applying AI and algorithms to real-world signals/comms, sensor fusion - London, hybrid working; to £58k plus benefits - You'll be helping to establish and further the state of the art, with a view to paving the way for future technology adoption and new applications.
)
Sitting within the site leadership team, the Laboratory Manager oversees all laboratory operations within a food-grade plastic recycling facility. Job Description: Laboratory Manager The Laboratory Manager plays a key role in supporting sustainable manufacturing processes while maintaining compliance with industry and regulatory standards. Department: Quality / Laboratory Operations - The manager leads a team of lab technicians, manages testing protocols, maintains compliance with relevant standards (e.g., FDA, EFSA,) and supports continuous improvement within the facility. Laboratory Operations & Testing - Develop, implement, and maintain laboratory testing methods, SOPs, and work instructions related to food-grade plastic recycling. Support risk assessments, corrective actions, and preventive measures related to laboratory and production processes.
Sitting within the site leadership team, the Laboratory Manager oversees all laboratory operations within a food-grade plastic recycling facility. Job Description: Laboratory Manager The Laboratory Manager plays a key role in supporting sustainable manufacturing processes while maintaining compliance with industry and regulatory standards. Department: Quality / Laboratory Operations - The manager leads a team of lab technicians, manages testing protocols, maintains compliance with relevant standards (e.g., FDA, EFSA,) and supports continuous improvement within the facility. Laboratory Operations & Testing - Develop, implement, and maintain laboratory testing methods, SOPs, and work instructions related to food-grade plastic recycling. Support risk assessments, corrective actions, and preventive measures related to laboratory and production processes.
)
This Chemistry Graduate role is ideal for an ambitious graduate looking to gain hands-on experience within a supportive school environment before undertaking teacher training. Are you a highly motivated and enthusiastic Chemistry Graduate looking to gain valuable school-based experience before progressing into teaching? A high-achieving secondary school in Havering is seeking a confident Chemistry Graduate to join their team as a Science Academic Mentor. As a Chemistry Graduate, you will support students across KS3KS5, delivering targeted 1:1 and small group interventions to help raise attainment and build confidence within Science. The successful Chemistry Graduate will work closely with teachers to support both high-achieving students and those requiring additional academic support, helping all learners to reach their full potential. Why choose this Chemistry Graduate role?
This Chemistry Graduate role is ideal for an ambitious graduate looking to gain hands-on experience within a supportive school environment before undertaking teacher training. Are you a highly motivated and enthusiastic Chemistry Graduate looking to gain valuable school-based experience before progressing into teaching? A high-achieving secondary school in Havering is seeking a confident Chemistry Graduate to join their team as a Science Academic Mentor. As a Chemistry Graduate, you will support students across KS3KS5, delivering targeted 1:1 and small group interventions to help raise attainment and build confidence within Science. The successful Chemistry Graduate will work closely with teachers to support both high-achieving students and those requiring additional academic support, helping all learners to reach their full potential. Why choose this Chemistry Graduate role?
The Medical Monitor will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. We are seeking several Medical Monitors to join our dynamic team. The Medical Monitor will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. All Medical Monitors have hybrid WFH flexibility. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. * Provide medical management and expertise for clinical trials; * Contribute medical expertise to study reports, regulatory documents, and manuscripts; * Coordinate with other departments in all phases of the studies and trials including feasibility ...
The Medical Monitor will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. We are seeking several Medical Monitors to join our dynamic team. The Medical Monitor will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. All Medical Monitors have hybrid WFH flexibility. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. * Provide medical management and expertise for clinical trials; * Contribute medical expertise to study reports, regulatory documents, and manuscripts; * Coordinate with other departments in all phases of the studies and trials including feasibility ...
NEW
We are seeking several Pharmaceutical Physicians to join our dynamic team in London. The Pharmaceutical Physician will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. The Pharmaceutical Physician will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. All Physicians have hybrid WFH flexibility. * Previous experience in pharmaceutical-related clinical research is preferred. We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Job Summary - Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. * Psychiatry
We are seeking several Pharmaceutical Physicians to join our dynamic team in London. The Pharmaceutical Physician will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. The Pharmaceutical Physician will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. All Physicians have hybrid WFH flexibility. * Previous experience in pharmaceutical-related clinical research is preferred. We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Job Summary - Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. * Psychiatry
NEW
The Clinical Research Associate at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. Our successful Clinical Research Associates possess varied backgrounds in medical and other science-related healthcare fields. * Site Coordinators, Clinical Research Coordinators * Communication with the medical site staff including coordinators, clinical research physicians and their site staff; * Assessing the clinical research sites patient recruitment and retention success and offering suggestions for improvement; Medpace is a full-service clinical contract research organization (CRO). For those with medical and/or health/life science interest and background who want to explore the research field, travel the UK, and be part of a team bringing ...
The Clinical Research Associate at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. Our successful Clinical Research Associates possess varied backgrounds in medical and other science-related healthcare fields. * Site Coordinators, Clinical Research Coordinators * Communication with the medical site staff including coordinators, clinical research physicians and their site staff; * Assessing the clinical research sites patient recruitment and retention success and offering suggestions for improvement; Medpace is a full-service clinical contract research organization (CRO). For those with medical and/or health/life science interest and background who want to explore the research field, travel the UK, and be part of a team bringing ...
NEW
)
Graduate Field Biologist (Pest Control)
Graduate Field Biologist (Pest Control)
Ernest Gordon Recruitment
Reading (RG1)
£26000 - £27000 per annum + Bonus + Commission + Car
Are you a Graduate with a background in Biology or Science looking for the opportunity to take your first step into industry with a company who are a proven market leader in their field, who provide excellent training to upskill their staff, clear progression pathways into senior management and a lucrative benefits package? This role would suit a Graduate with a background in Biology or Science looking for their first role in a thriving company, who prioritise their staff, offering long term progression, industry leading training and the ability to boost your earnings with overtime and commission. * Biology or Science Graduate Keywords: Pest, Prevention, Management, Consultancy, Pest Control, Biology, Science, Life Science, Biologist, Field, Reading, Swindon, Uxbridge, Andover, Basingstoke £26,000 - £27,000 + Bonus + Commission + Car + Training + Progression + Benefits
Are you a Graduate with a background in Biology or Science looking for the opportunity to take your first step into industry with a company who are a proven market leader in their field, who provide excellent training to upskill their staff, clear progression pathways into senior management and a lucrative benefits package? This role would suit a Graduate with a background in Biology or Science looking for their first role in a thriving company, who prioritise their staff, offering long term progression, industry leading training and the ability to boost your earnings with overtime and commission. * Biology or Science Graduate Keywords: Pest, Prevention, Management, Consultancy, Pest Control, Biology, Science, Life Science, Biologist, Field, Reading, Swindon, Uxbridge, Andover, Basingstoke £26,000 - £27,000 + Bonus + Commission + Car + Training + Progression + Benefits
FEATURED
)
A UKAS accredited Asbestos specialist is recruiting for a detail-oriented Asbestos Lab Analyst in the South East of England. Job Title: Asbestos Lab Analyst -Successful record working as an Asbestos Lab Analyst Alternative job titles: Asbestos Analyst, Asbestos Bulk Analyst. We have a large dedicated team, with over 25 years combined industry experience within Asbestos recruitment specifically geared to dealing with Asbestos Surveyors/Analysts/Lab Technicians, Administrators, Project/Regional /Technical/Quality/Training/Sales Managers through to Director Level for both Consultancy & Removal. -Receiving samples into the lab, logging and storing correctly -Calibrating lab equipment - Future Select are the leading market supplier for recruitment in the Asbestos industry; we work with the best clients and candidates and supply the majority of permanent jobs in the asbestos market.
A UKAS accredited Asbestos specialist is recruiting for a detail-oriented Asbestos Lab Analyst in the South East of England. Job Title: Asbestos Lab Analyst -Successful record working as an Asbestos Lab Analyst Alternative job titles: Asbestos Analyst, Asbestos Bulk Analyst. We have a large dedicated team, with over 25 years combined industry experience within Asbestos recruitment specifically geared to dealing with Asbestos Surveyors/Analysts/Lab Technicians, Administrators, Project/Regional /Technical/Quality/Training/Sales Managers through to Director Level for both Consultancy & Removal. -Receiving samples into the lab, logging and storing correctly -Calibrating lab equipment - Future Select are the leading market supplier for recruitment in the Asbestos industry; we work with the best clients and candidates and supply the majority of permanent jobs in the asbestos market.
FEATURED
Medical Affairs Lead
Medical Affairs Lead
UKPharm Limited
City of London (EC1)
Up to £110,000 per annum bonus and full benefits package
Medical Lead (final signatory) - Pharmaceutical - London - You will have good experienced turning medical evidence into into clear, clinically-sound value narratives, leading medical strategy and being the trusted medical partner for all commercial functions. A fantastic opportunity to enter one of the most buoyant pharmaceutical markets in the UK at present in a consistent state of rapid growth both in turnover and their structure. The role would be office based three days a week in London. They offer a strong package plus bonus in addition to a good peripheral package including such as pension and healthcare.
Medical Lead (final signatory) - Pharmaceutical - London - You will have good experienced turning medical evidence into into clear, clinically-sound value narratives, leading medical strategy and being the trusted medical partner for all commercial functions. A fantastic opportunity to enter one of the most buoyant pharmaceutical markets in the UK at present in a consistent state of rapid growth both in turnover and their structure. The role would be office based three days a week in London. They offer a strong package plus bonus in addition to a good peripheral package including such as pension and healthcare.
Taking accountability, as part of a team of Biotechnologists, for the successful manufacture of viral vector batches - Join Us in Changing Lives - AtOXB, our people are at the heart of everything we do. Were on a mission to enable life-changing therapies to reach patients around the worldand were looking for passionate individuals who embody our core values every day:Responsible, Responsive, Resilient, and Respectful. Were currently recruiting for an experienced Biotechnologistto join ourManufacturing team. In this role, you will support the Team Lead by coordinating the teams daily production activities and contributing to the manufacturing of GMP viral vectors, playing a key part in advancing our mission and making a real difference. * Ensuring that all work within the manufacturing facility is carried out in compliance with the facilities GMP procedures
Taking accountability, as part of a team of Biotechnologists, for the successful manufacture of viral vector batches - Join Us in Changing Lives - AtOXB, our people are at the heart of everything we do. Were on a mission to enable life-changing therapies to reach patients around the worldand were looking for passionate individuals who embody our core values every day:Responsible, Responsive, Resilient, and Respectful. Were currently recruiting for an experienced Biotechnologistto join ourManufacturing team. In this role, you will support the Team Lead by coordinating the teams daily production activities and contributing to the manufacturing of GMP viral vectors, playing a key part in advancing our mission and making a real difference. * Ensuring that all work within the manufacturing facility is carried out in compliance with the facilities GMP procedures
PREMIUM
Position: Associate Analytical Chemist, Quality Control Were looking for a proactive and detail-oriented Associate Analytical Chemist to join our Chemistry Quality Control team at our Rushden site. With over 21,000 employees worldwide across 23 locations in the US, UK and China, we support drug discovery through to manufacturing with fully integrated, high-quality services. In this role you will support laboratory operations through routine and specialised analytical tasks including carrying out scheduled calibration and verification of instruments, documenting all activities in line with GMP and internal SOPs. * Perform scheduled calibration and verification of analytical instruments (e.g., pipettes, balances). * BSc Chemistry, Analytical Chemistry or closely related discipline * Practical laboratory skills with experience within an Analytical laboratory desirable
Position: Associate Analytical Chemist, Quality Control Were looking for a proactive and detail-oriented Associate Analytical Chemist to join our Chemistry Quality Control team at our Rushden site. With over 21,000 employees worldwide across 23 locations in the US, UK and China, we support drug discovery through to manufacturing with fully integrated, high-quality services. In this role you will support laboratory operations through routine and specialised analytical tasks including carrying out scheduled calibration and verification of instruments, documenting all activities in line with GMP and internal SOPs. * Perform scheduled calibration and verification of analytical instruments (e.g., pipettes, balances). * BSc Chemistry, Analytical Chemistry or closely related discipline * Practical laboratory skills with experience within an Analytical laboratory desirable
NEW